1383467-74-0

Basic information

• Product Name: 3-(naphthalene-4-yl)-2-(phenylthio)propanal
• Synonyms: 3-(naphthalene-4-yl)-2-(phenylthio)propanal
• CAS NO: 1383467-74-0
• Molecular Weight: 292.401
• Mol File: 1383467-74-0.mol

Chemical Properties

• CAS DataBase Reference: 3-(naphthalene-4-yl)-2-(phenylthio)propanal(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(naphthalene-4-yl)-2-(phenylthio)propanal(1383467-74-0)
• EPA Substance Registry System: 3-(naphthalene-4-yl)-2-(phenylthio)propanal(1383467-74-0)

Safety Data

• Hazardous Substances Data: 1383467-74-0(Hazardous Substances Data)

Upstream product

• 16176-22-0 3-(naphthalene-1-yl)prop-2-yn-1-ol 
• 108-98-5 thiophenol 
• 1224466-33-4 D-3-phenylprop-2-yn-1-ol 

Relevant articles and documents

PREPARATION OF [ALPHA]-SULFENYLATED CARBONYL COMPOUNDS FROM PROPARGYLIC ALCOHOLS IN ONE STEP

The present relates to a method and a kit to produce an optically pure α-sulfenylated carbonyl compound comprising a primary or a secondary propargylic alcohol and an aryl thiol, a transition metal catalyst and a solvent.

Atom-efficient gold(I)-chloride-catalyzed synthesis of α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols: Substrate scope and experimental and theoretical mechanistic investigation

Gold(I)-chloride-catalyzed synthesis of α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols showed a wide substrate scope with respect to both propargylic alcohols and aryl thiols. Primary and secondary aromatic propargylic alcohol

A gold(I)-catalyzed route to α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols

A one-step atom efficient gold(i)-catalyzed route to α-sulfenylated ketones and aldehydes from propargylic alcohols and aryl thiols is described.